Abstract

Patients with advanced AML, ie, those not in first (CR1) or second complete remission (CR2) have poor outcome and are considered poor transplant candidates. The purpose of this study was to identify a subgroup of patients with active disease at the time of transplant that benefits from allogeneic transplantation. Between 2005 and 2013, 782 patients underwent allogeneic transplant from a fully matched (10/10) related or unrelated donor at our center. Of these 361 patients with advanced disease, defined as patient not in CR1 or CR2, were included in this analysis. Cox proportional hazards regression analysis was used for univariate and multivariate analysis to predict overall survival. Variables considered in the analysis were age, sex, SWOG cytogenetics risk group, BM and PB blast%, regimen intensity (myeloablative v/s reduced intensity) and type of AML (de novo, secondary to MDS or MPD or therapy related AML). At a median follow up of 26 months in the surviving patients, OS, PFS, NRM and relapse rate were 26%, 24%, 23% and 48%, respectively. In a univariate analysis poor risk cytogenetics (P<0.001) and bone marrow blasts >4% (P 0.006) or any blasts in peripheral blood (P<.001) indicated adverse outcome for OS. When poor risk cytogenetics and peripheral and/or bone marrow blasts were considered simultaneously (Table 1, fig 1), significantly superior survival was observed in patients with less than 5% BM blasts without any circulating blast and good or intermediate risk cytogenetics. This impact was also seen for PFS and disease progression. At 3 years PFS and OS were 44% and 46% in this subgroup.Tabled 1NOutcomes at 3 yearsProgressionPPFSPOSPBad Risk Cytogenetics/ Blasts BM >4% or PB blast >0% No / No7735%Ref.44%Ref.46%Ref. Yes / No3139%0.128%0.0230%0.01 No / Yes11750%0.00221%<0.00123%<0.001 Yes / Yes11057%<0.00114%<0.00116%<0.001 Open table in a new tab Patients with low blast counts in the absence of poor-risk cytogenetics should be considered for transplant, even if they are not in remission.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.